Take Back My Life

Take Back My Life Musings, raw refections, advocacy, healing and examining according to my moral compass My name is Briana Beaver, and I'm taking back my life!

I have been overcoming extreme and extraordinary obstacles since my birth. An hour after I was born, I died. I was resuscitated, but the event left me with permanent brain damage, resulting in Cerebral Palsy. When I was 9 years old, I mysteriously started to experience health problems that included gastrointestinal, pulmonary, metabolic, and neurological symptoms. But I never let this stop me. I p

ursued my passions, and did my best to live a normal life. I graduated high school in 3 years, and in 2011 I graduated from Chico State, Summa Cum Laude, with a degree in Sociology. It was then that my health became even worse. The pain became horrifically intense. I had extreme sensory overload, so that every stimulus - sight, sound, and smell - everything caused pain. I was so mysteriously debilitated that I was unable to eat or drink. By summer 2012 I was in Stanford Hospital, wasted away to 75 lbs. The pain was so torturous that I welcomed the thought of death. In December of 2014, my medical mystery was finally given a name: Lyme Disease. Since then, I have undergone an extremely expensive battery of treatments, none of which are covered by insurance. I have improved, but I’m still incredibly medically fragile. I’m currently unable to read for more than 10 minutes at a time, and can’t use a computer or TV for any length at all. I had to dictate this message because I’m unable to write it myself. However, I desperately needed to share how deeply I’m committed to moving forward. It’s time for me to FINALLY take back my life! My family is organizing the Take Back My Life campaign to help pay for the extremely expensive treatments Briana direly needs, but isn’t covered by insurance. For more information on Briana’s journey to health, and to donate toward her treatment, visit:

http://gofund.me/pvpq2k

To better understand the devastating and debilitating symptoms of Lyme Disease, please visit www.lymedisease.org/

What if patients were teaching medical school?Well, here goes…The perspective and personal narratives of people on the r...
09/14/2026

What if patients were teaching medical school?

Well, here goes…

The perspective and personal narratives of people on the receiving end of medicine matters. That’s why I’m so thrilled to have the evolving partnership of a doctor who understands, appreciates and more importantly, takes action upon this truth.

I never imagined myself being in a position to educate future doctors, but that’s where I find myself.

Dr. Schnell told me that he is in charge of teaching shared-decision making to a number of residents and he plans to include Care Cards as part of the curriculum. He told me he welcomes my input about how best to do this and what the most important points are to relay to these new doctors.

Wow. That’s a lot to unpack, right? If I could bottle a lifetime of demeaning, demoralizing and harmful medical experiences into a tangible message for hope, improvement and a new frontier of healing, what would that look like?

This is something I will be thinking about as the collaboration unfolds and we decide together how I can be a part of shaping doctors’ minds and more importantly, hearts.

When I was a little girl, I knew I would get married someday.I knew it the way most kids know things; with the kind of w...
09/11/2026

When I was a little girl, I knew I would get married someday.

I knew it the way most kids know things; with the kind of wild abandon that doesn’t need to consult logistical arrangements. I had a precise understanding that I would spend my adult life with a kind hearted, easy-going man named “Toby.“

He would respect my professional aspirations, which, at that time included being both a pediatrician and a marine biologist. We would enjoy a frenetic, deeply loving life with three daughters, the youngest of which would be adopted.

And that would be the way it was.

I also knew that people thought I was different. I observed how other children watched me with what began as curiosity and later became something much more damaging: fear. But I never thought this would preclude me from being who I wanted to be: a wife, a mother, a professional.

To be honest, I never really realized that men didn’t notice me in the way that women want to be noticed until college. It began to dawn on me that although I had so painstakingly created a life where I was “included“ like everybody else, I remained invisible in many ways. I did my best to entice the few crushes I got close to as friends into something more, even going so far as to help routinely one friend with his homework. To no avail. I remained the perpetual, as*xual friend.

I went so far as to design and implement a voluntary honors thesis about s*xuality and disability. I subconsciously thought that perhaps, if I wasn’t the only person with a disability being sidelined romantically, maybe I would feel like less of a weirdo. I thought that perhaps the data I collected could be used to help educate, illuminate and dismantle all of the terrible things we tell each other about perceived differences.

I believed that perhaps this information could help us evolve, bolster humanity, dismantle stereotypes and hell, maybe, help me get a date.

Although I can’t say that I know any man who would be tickled by reading academic data, I did what I could given the resources and talents I had. With virtually no experience with romance, I counted on my intellectualism to hopefully pave the way to a meaningful connection with a man.

When that didn’t work, I tried harder to be loved. And I’ve been trying harder my whole damn life.

So where is “Toby“?

So now I’m 38 years old and I still want to be a mother, a wife and a meaningful partner in a long lasting relationship. To say that I’ve exhausted my internal and external resources to have a chance at experiencing my childhood expectations, would be an understatement.

Would it be erroneous for me to believe that I am single because I have a disability? Has the research I’ve done on these topics penetrated my psyche to such a degree that I am overthinking the impact of my perceived differences on men?

Yes and no.

I’ve become aware that trying harder is not the solution. In fact, it is representative of the very problem that underlies the core of my research. People with disabilities are socialized to believe that they are inherently wrong, broken and need to compensate in order to be loved.

There’s no question about whether or not I’ve spent a lifetime attempting to compensate. Clearly, I have.

So, where do I go from here? How do I have an opportunity to have a wonderful, loving partnership with a man when there are so many societal and logistical barriers? There are no easy answers to these questions and unlike many of my other posts, this is not a linear narrative. I don’t have an answer, a hopeful crush waiting in the wings, or some other way to wrap this package up in a pretty bow.

All I can say is that I’ve learned from my own academic research and my personal experiences that there is a lot of damaging misinformation out there about disability and s*xuality, in fact, you can read all about it in my book.

In the meantime, here’s my PSA:

Yes, I can have s*x. (It’s not painful or scary. I’ve done it before any everything was just peachy.)
No, my disability is not genetic.
Yes, I can have a baby.
Yes, I can be a parent.

That’s all for now!

(Please note: I’m not looking for advice for different things to try. If anything, my point is that the TRYING HARDER is part of the problem, it’s not the solution.

Also, if you think “Toby“ could be your son, nephew, brother or friend, please let me know!)

It hit me today that I’m in a one-of-a-kind position that most people probably have never been in or never will be…An op...
09/11/2026

It hit me today that I’m in a one-of-a-kind position that most people probably have never been in or never will be…

An opportunity to partner with a doctor to implement a patient-created resource in a hospital setting.

I don’t work for a healthcare corporation, medical industry, quality assurance or any bureaucratic watchdog initiating policies for the sake of buoying faceless stakeholders.

I am a person. I am a patient. I am an advocate and I care.

So, given all of the above, I have a wonderful learning opportunity and collaborative journey ahead. I will be documenting this process as best as I can so I can reflect and glean every speck of insight and wisdom as we go.

UT Texas Health, here we come!

Introducing Our Service Dog Care Card!Service Dogs Make a Difference 🐾A service dog is more than a pet—they are a highly...
09/10/2026

Introducing Our Service Dog Care Card!

Service Dogs Make a Difference 🐾

A service dog is more than a pet—they are a highly trained working partner who helps their handler navigate daily life with greater safety, independence, and confidence.

Our Service Dog Care Card offers simple, friendly reminders about how to interact respectfully with both the service dog and the person they support.

It’s designed to encourage awareness, kindness, inclusion, and good human interaction without judgment or shame.

https://www.etsy.com/listing/4572411337/service-dog-care-card?ref=shop_home_active_1&dd=1&logging_key=74d76f2e8d68456141d8fd905d53b45fb95a017e%3A4572411337

I’m not running for office but it was a real treat to see my Care Cards poster proudly displayed at the Butte County Dem...
09/09/2026

I’m not running for office but it was a real treat to see my Care Cards poster proudly displayed at the Butte County Democratic Party Headquarters! Thank you so much to Regional Director William Monroe for your support and all of the great work you are doing!

Celebrating one year of writing for North State Parent Magazine!I'm grateful to work for a publication where my authenti...
09/08/2026

Celebrating one year of writing for North State Parent Magazine!

I'm grateful to work for a publication where my authentic voice is represented, appreciated and shared across the north-state! I'm looking forward to another year!

The Summer Care Cards poster tour has been a great success!This has been a wonderful tool not only to introduce CC to my...
09/06/2026

The Summer Care Cards poster tour has been a great success!

This has been a wonderful tool not only to introduce CC to my community and beyond, but also to spread awareness and educational training about this resource and how it might be used. I’m so thankful to local businesses, medical clinics and hospitals that have lended support by featuring the poster at their location!

Thank you to:

Dr. Jennifer Hawes
Postal Plus
Shalom Free Clinic
ABC Books
Mayers Memorial Hospital
Butte County Democratic Party
Magnolia Gift & Garden
Butte County Library
Kasandra Kapel
International Society of Shared-Decision Making

+ more!

Thank you to Wilson Printing for donating these beautiful posters!

Small cards. Big ripple of love!

Don’t you just love a good story of unexpected coincidence?My dear friend Audri has been working behind the scenes to su...
09/06/2026

Don’t you just love a good story of unexpected coincidence?

My dear friend Audri has been working behind the scenes to support me with Care Cards since day one. From computer assistance with the original first cards design logistics to technical support with applying to the Dartmouth conference, she’s been an integral part of the team. How ironic is it then that I happened to connect with an ER doctor at an international conference who practices in her hometown?

I’m so delighted that the first Care Cards hospital pilot program will be close to my dear friend’s neighborhood! UT Health Texas here we come!

Address

1010 Mangrove Ave Ste D Chico, California 95926
Chico, CA

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